Regulatory Information Management

Optimize and control the management of highly regulated business processes for worldwide submissions and approvals to accelerate the delivery of safest, most efficacious devices to market.

Gaining the right product approvals and certificates for major markets is fundamental to both succeed and to ensure safety and effectiveness of every medical device. Properly defined and prepared submission reports help assure that the submission contains the appropriate defined information requested by the various regulatory bodies for the specific product classification. For example, the collection of products and key UDI attributes from a company’s systems can be automatically bulked to refine and reuse data for UDI submission and approvals.

Regulatory Information Management breaks the silo barriers within a company to create a more unified approach to launching a product to market, therefore significantly decreasing time to market. It allows companies to eliminate scattered processes and data and to “embed” regulations as an asset, optimizing and controlling the management of highly-regulated business processes for worldwide submissions and approvals.